Related Experiment Video
Updated: Sep 27, 2026

An Air-liquid Interface Bronchial Epithelial Model for Realistic, Repeated Inhalation Exposure to Airborne Particles for Toxicity Testing
Published on: May 13, 2020
Inflammatory effects of inhaled endotoxin-contaminated metal working fluid aerosols in rats
Michael P DeLorme1, Xiufeng Gao, Nicole Doyon-Reale
1Department of Occupational and Environmental Health Sciences, Wayne State University, Detroit, Michigan, USA. michael.p.delorme@usa.dupont.com
Abstract:
Exposure to aerosols generated from water-soluble metal-working fluids (MWF) is associated with numerous respiratory symptoms consistent with an acute pulmonary inflammatory event. Previous studies in mice and guinea pigs have implicated endotoxin contamination of MWF as the causative agent responsible for inducing pulmonary neutrophilia and decrements in airway conductance. However, little information is known about the relationship between endotoxin-contaminated MWF exposure and changes in airway physiology. The present study, utilizing a rat model, has demonstrated that exposure to 10 mg/m3 with endotoxin (0 to 3.2 micrograms/m3) resulted in a time- and concentration-dependent migration of neutrophils in the lung tissue's interstitial spaces as well as the lavageable airways. In contrast to other airborne toxicants, where neutrophil infiltration of the lung has been associated with hyperresponsive airways, the endotoxin-induced neutrophilia observed in the present study was not associated with airway hyperresponsiveness to challenge with the muscarinic agent methacholine or with permeability damage to the lung. Bronchoalveolar lavage (BAL)-recovered neutrophils demonstrated no adverse effects as a result of endotoxin-contaminated MWF exposure. In contrast, a population of alveolar macrophages was observed to be enlarged in size and demonstrated an increased sensitivity to oxidative metabolism when challenged with phorbol myristate acetate, consistent with being at a relatively high state of activation. These results suggest that while endotoxin contamination of MWF is capable of producing an acute inflammatory event, other predisposition factors may be required to induce alterations in pulmonary physiology.
Insights
Exposure to metal-working fluid aerosols containing endotoxin causes lung inflammation and activates alveolar macrophages in rats. However, this exposure did not lead to airway hyperresponsiveness or lung damage, suggesting other factors may be needed for significant pulmonary changes.
Area of Science:
- Occupational Health
- Pulmonary Toxicology
- Immunology
Background:
- Aerosols from metal-working fluids (MWF) are linked to respiratory issues.
- Endotoxin contamination in MWF is suspected to cause lung inflammation and airway changes.
- Limited data exists on endotoxin-MWF exposure effects on airway physiology.
Purpose of the Study:
- To investigate the impact of endotoxin-contaminated MWF aerosol exposure on rat airway physiology.
- To determine if MWF-induced neutrophilia correlates with airway hyperresponsiveness.
- To assess the activation state of immune cells in the lungs post-exposure.
Main Methods:
- Rats were exposed to MWF aerosols with varying endotoxin concentrations.
- Pulmonary inflammation was assessed via neutrophil migration in lung tissue and lavage fluid.
- Airway responsiveness was measured using methacholine challenge.
- Alveolar macrophages were analyzed for size and oxidative metabolism.
Main Results:
- Endotoxin-contaminated MWF exposure caused a time- and dose-dependent neutrophil migration into lung tissues and airways.
- Neutrophilia was not associated with increased airway hyperresponsiveness or lung permeability damage.
- Alveolar macrophages enlarged and showed increased oxidative metabolism, indicating activation.
- Bronchoalveolar lavage-recovered neutrophils showed no adverse effects.
Conclusions:
- Endotoxin in MWF aerosols induces acute lung inflammation and macrophage activation in rats.
- MWF-induced inflammation does not directly cause airway hyperresponsiveness.
- Additional factors may be necessary to trigger significant pulmonary physiological alterations from MWF exposure.

